A Reinvestigation of the Oxidative Rearrangement of Yohimbane-Type Alkaloids. Part A. Formation of pseudoindoxyl ( = 1,2-dihydro-3H-indol-3-one) derivatives-Reference-Cited by-同舟云学术

A Reinvestigation of the Oxidative Rearrangement of Yohimbane-Type Alkaloids. Part A. Formation of pseudoindoxyl ( = 1,2-dihydro-3H-indol-3-one) derivatives

Published:1994-08-10 Issue:5 Volume:77 Page:1331-1345
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Stahl Reto,Borschberg Hans-J�rg

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference32 articles.

1. Synthesis of Aristotelia-Type Alkaloids. Part XII. Total synthesis of (−)-tasmanine. Stereoelectronic factors that control the rearrangement of 3H-indol-3-ol derivatives to oxindoles ( = 1,3-dihydro-2H-indol-2-ones) or to pseudoindoxyls ( =1,2-dihydro-3H-

2. Studies on Uncaria Alkaloid. XVIII. Structure of Uncarine. (13). Structure of Uncarine-A and Uncarine-B.

3. THE STRUCTURE AND STEREOISOMERISM OF THREE MITRAGYNA ALKALOIDS

4. 3-Hydroxymethyleneoxindole and its Derivatives

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